Abstract
Plasmonic materials are intensively used to extend the photoactivity of large bandgap semiconductors into the visible light region. In this framework, the present study examines the joint role played by the morphology and composition of plasmonic nano particles in their photosensitizing capabilities. The critical influence of these parameters is evidenced by the effect of Au and core-shell Au@Ag nanorods on a TiO2-driven photochemical probe reaction. In this case, the use of the bimetallic composites leads to a remarkable increase in the photocatalytic activity of the semiconductor compared to that found for the monometallic Au sensitizers. The mechanism behind this observation has then been computed theoretically concluding that, in terms of hot electron injection, the contribution of the transversal modes of the Au@Ag NRs and the low damping of these nanostructures are responsible for the photocatalytic properties reported herein. The great potential of these architectures is confirmed by their notable performance toward photocatalytic hydrogen generation, rendering this approach an appealing strategy in the search for efficient solar-driven energy systems.
Dokumententyp: | Zeitschriftenartikel |
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Fakultät: | Physik |
Themengebiete: | 500 Naturwissenschaften und Mathematik > 530 Physik |
ISSN: | 2380-8195 |
Sprache: | Englisch |
Dokumenten ID: | 89224 |
Datum der Veröffentlichung auf Open Access LMU: | 25. Jan. 2022, 09:29 |
Letzte Änderungen: | 25. Jan. 2022, 09:29 |